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93869-53-5

bis(2-bromophenyl)(phenyl)phosphane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93869-53-5 Structure

  • Basic information

    1. Product Name: bis(2-bromophenyl)(phenyl)phosphane
    2. Synonyms: bis(2-bromophenyl)(phenyl)phosphane
    3. CAS NO:93869-53-5
    4. Molecular Formula:
    5. Molecular Weight: 420.083
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93869-53-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: bis(2-bromophenyl)(phenyl)phosphane(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(2-bromophenyl)(phenyl)phosphane(93869-53-5)
    11. EPA Substance Registry System: bis(2-bromophenyl)(phenyl)phosphane(93869-53-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93869-53-5(Hazardous Substances Data)

93869-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93869-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93869-53:
(7*9)+(6*3)+(5*8)+(4*6)+(3*9)+(2*5)+(1*3)=185
185 % 10 = 5
So 93869-53-5 is a valid CAS Registry Number.

93869-53-5Relevant articles and documents

Dynamic Conformational Behavior in Stable Pentaorganosilicates

van der Boon, Leon J. P.,Hendriks, Jesper H.,Roolvink, Danny,O'Kennedy, Sean J.,Lutz, Martin,Slootweg, J. Chris,Ehlers, Andreas W.,Lammertsma, Koop

, p. 3318 - 3328 (2019)

Silicates with five organic groups are conformationally dynamic even with two bidentate ligands. Symmetry breaking by incorporating a single nitrogen or phosphorus atom provides insight into their dynamic behavior. N-containing silicates with bidentate 2-

Dibenzophosphaborin: A hetero-π-conjugated molecule with fluorescent properties based on intramolecular charge transfer between phosphorus and boron atoms

Agou, Tomohiro,Kobayashi, Junji,Kawashima, Takayuki

, p. 4373 - 4376 (2007/10/03)

(Chemical Equation Presented) The first dibenzo-1,4-phosphaborins were synthesized and characterized by X-ray crystallographic analysis. The phosphaborins exhibited UV/vis absorption derived from intramolecular charge transfer from the phosphorus atom to

Water soluble phosphines Part XV. Syntheses of multiply functionalized and chiral phospine ligands by Pd-catalyzed P-C and C-C coupling reactions

Brauer, David J.,Hingst, Martin,Kottsieper, Konstantin W.,Liek, Christian,Nickel, Thomas,Tepper, Michael,Stelzer, Othmar,Sheldrick, William S.

, p. 14 - 26 (2007/10/03)

Phosphine ligands containing mono- and multiply substituted aromatic substituents (1-13, 19a and 19b) are accessible in high yields by palladium-catalyzed P-C coupling reactions between primary, secondary or disecondary phosphines and iodo- or bromoaromatic compounds. The reaction is of broad applicability and compatible with electron donor or electron acceptor substituents in ortho, meta or para position to the halogen in the aromatic ring systems. It may be performed in protic and aprotic solvents. The chiral spirocyclic boronato complex 15a is formed upon reaction of 3 with boric acid, while with benzeneboronic acid 15c with a peripheral Lewis acid group is obtained. The Pd-mediated P-C coupling reaction of primary phosphines proceeds stepwise, tailor-made chiral secondary (16) and tertiary phosphines (17) being formed in high yield. Through combination with Suzuki-type C-C coupling reactions, the scope of Pd-catalyzed P-C coupling may be extended further, novel ligands (20a, 20b, 21a, 21b) with biphenylyl substituents being accessible. The X-ray structures of the salicylic acid derivative 3 (space group P1) and of ortho-iso-propylphenyl-diphenylphosphine 6 (space group Pbca) have been determined.

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